Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4746868 | 5820983 | F | 4746868-0 | 20050601 | 20050609 | 20050817 | EXP | PHBS2005BE08252 | NOVARTIS PHARMACEUTICALS CORP. | 47 | YR | F | Y | 20050816 | MD | BELGIUM |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4746868 | 1006328787 | PS | ZOMETA | 1 | INTRAVENOUS | 4 MG, QMO | 21223 | ||||
| 4746868 | 1006328788 | C | FLUOROURACIL + CYCLOPHOSPHAMIDE | 2 | UNKNOWN | ||||||
| 4746868 | 1006328789 | C | EPIRUBICIN | 1 | UNKNOWN | ||||||
| 4746868 | 1006328790 | C | TAXOTERE | 1 | UNKNOWN | EVERY 3 TO 4 WEEKS | |||||
| 4746868 | 1006328791 | C | MEDROL | 1 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4746868 | 1006328787 | METASTASES TO BONE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4746868 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4746868 | ASEPTIC NECROSIS BONE |
| 4746868 | WOUND DEBRIDEMENT |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4746868 | 1006328787 | 20040301 | 20050501 | ||
| 4746868 | 1006328788 | 20040301 | 20040401 | ||
| 4746868 | 1006328789 | 20040301 | 20040401 | ||
| 4746868 | 1006328790 | 20040401 | 20041201 | ||
| 4746868 | 1006328791 | 20040401 | 20041201 |